PERCEVAL S Valve Clinical Study for Chinese Registration (PERFECT)

Corcym

Status

Active, not recruiting

Conditions

Aortic Valve Stenosis

Aortic Valve Disease

Treatments

Device: Aortic Valve Replacement with Perceval S sutureless heart valve

Study type

Interventional

Funder types

Industry

Identifiers

NCT03481387

TPS004

Details and patient eligibility

About

This is a prospective, open, single arm, multi-center clinical study in China. The primary objective of this study is to demonstrate the safety and effectiveness of the PERCEVAL S heart valve when used to replace a diseased native or malfunctioning prosthetic aortic valve in the indicated Chinese population for tissue heart valve replacement and suitable to the PERCEVAL S valve.

The secondary objectives are to collect all relevant device and subject demographics, procedural and hospital discharge, short and long-term data, as described in the secondary endpoints section.

Enrollment

61 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subject of age > 60 years.
Subject with aortic valve stenosis or steno-insufficiency.
Subject has signed the informed consent.
Subject in which preoperative evaluation is indicated for the need of native or prosthetic aortic valve replacement via open heart surgery
Subject is located in a geographic location that will enable the subject to return to the study site for follow-up examinations (i.e. geographically stable).

Exclusion criteria

Subject has preexisting valve prosthesis or annuloplasty rings in the mitral, pulmonic or tricuspid position.
Subject requires a double or multiple valve replacement or repair of the mitral, tricuspid, or pulmonic valve.
Subject requiring simultaneous cardiac procedures, apart from septal myectomy and/or coronary by-pass graft (CABG).
Subject has active endocarditis.
Subject has active myocarditis
Subject has aneurysmal dilation or dissection of the ascending aortic wall.
Subject is drug abuser, alcohol abuser, prison inmate, institutionalized, or is unable to give informed consent.
Subject has a major or progressive non-cardiac disease that, in the investigator's experience, results in a life expectancy of less than 1 year, or the implant of the device produces an unacceptable increased risk to the subject.
Subject with known hypersensitivity to nickel alloys.
Subject is undergoing renal dialysis for chronic renal failure or has hyperparathyroidism.
Subject has had an acute preoperative neurological deficit, myocardial infarction, or cardiac event that has not returned to baseline or stabilized for ≥30 days prior to the planned valve implant surgery.
Subject is known to be noncompliant or is unlikely to complete the study.
Subject with an aortic root enlargement, where the ratio between the diameter of the STJ and the annulus diameter, assessed by TEE, is > 1.3. Or for other anatomical reasons that not suitable for PERCEVAL S per IB.